JPH0333267A - Finishing oil for treating thermoplastic synthetic fiber - Google Patents
Finishing oil for treating thermoplastic synthetic fiberInfo
- Publication number
- JPH0333267A JPH0333267A JP16288189A JP16288189A JPH0333267A JP H0333267 A JPH0333267 A JP H0333267A JP 16288189 A JP16288189 A JP 16288189A JP 16288189 A JP16288189 A JP 16288189A JP H0333267 A JPH0333267 A JP H0333267A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- thermoplastic synthetic
- ester
- formula
- oil
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920002994 synthetic fiber Polymers 0.000 title claims description 17
- 239000012209 synthetic fiber Substances 0.000 title claims description 17
- 229920001169 thermoplastic Polymers 0.000 title claims description 15
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 16
- 150000002148 esters Chemical class 0.000 claims abstract description 13
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 9
- 229930195729 fatty acid Natural products 0.000 claims abstract description 9
- 239000000194 fatty acid Substances 0.000 claims abstract description 9
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 7
- 239000000126 substance Substances 0.000 claims abstract description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 abstract description 6
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 abstract description 5
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 abstract description 2
- 239000005639 Lauric acid Substances 0.000 abstract description 2
- 235000021355 Stearic acid Nutrition 0.000 abstract description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 abstract description 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 abstract description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract description 2
- 239000008117 stearic acid Substances 0.000 abstract description 2
- 230000000391 smoking effect Effects 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 23
- 238000000034 method Methods 0.000 description 12
- -1 Fatty acid esters Chemical class 0.000 description 9
- 238000012545 processing Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000779 smoke Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- GSAHAZJWNMHSNI-UHFFFAOYSA-N 2,2-bis(dodecanoyloxymethyl)butyl dodecanoate Chemical class CCCCCCCCCCCC(=O)OCC(CC)(COC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC GSAHAZJWNMHSNI-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- OXPCWUWUWIWSGI-MSUUIHNZSA-N Lauryl oleate Chemical compound CCCCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC OXPCWUWUWIWSGI-MSUUIHNZSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- QZULIRBSQUIUTA-CLFAGFIQSA-N bis[(z)-octadec-9-enyl] hexanedioate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCC\C=C/CCCCCCCC QZULIRBSQUIUTA-CLFAGFIQSA-N 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012261 resinous substance Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- 239000010913 used oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野〕
本発明は熱可塑性合成繊維処理用油剤、特に加熱工程を
経る熱可塑性合成繊維処理用油剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to an oil agent for treating thermoplastic synthetic fibers, and particularly to an oil agent for treating thermoplastic synthetic fibers that undergoes a heating step.
従来熱可塑性合成繊維を製造する場合、溶融紡糸法によ
り紡出した糸条を延伸するために加熱したり、性質改善
のために熱固定が行われる。Conventionally, when producing thermoplastic synthetic fibers, yarns spun by a melt-spinning method are heated to draw them or heat-set to improve their properties.
また、仮撚加工工程を経る熱可塑性台tc繊維の場合に
は形態固定のために熱処理されるのが一般的であり、タ
イヤコード糸の如き産業資材に供される合成繊維に対し
ては、高強度糸を得るために過酷な加熱条件のもとて延
伸されるのが通例である。各種製造工程において、繊維
糸条はかなりの高速で処理されることが多く、紡糸、延
伸、加工等の工程を円滑に進めることを目的として繊維
糸条に処理される処理油剤に対し、高度の耐熱性、平滑
性、制電性が要求されている。In addition, in the case of thermoplastic TC fibers that undergo a false twisting process, they are generally heat treated to fix their shape, and for synthetic fibers used in industrial materials such as tire cord yarn, It is customary to draw under harsh heating conditions to obtain high strength yarns. In various manufacturing processes, fiber threads are often processed at fairly high speeds, and processing oils used on fiber threads are processed at high speeds in order to smoothly proceed with processes such as spinning, drawing, and processing. Heat resistance, smoothness, and antistatic properties are required.
これらの要求を満足させるために、従来から乳化剤、帯
電防止剤等と配合する潤滑剤成分として、鉱物油や高級
アルコールと脂肪酸とのエステル類、アジピン酸やセバ
シン酸等の二塩基酸とのエステル類、トリメチロールプ
ロパン、グリセリン等の多価アルコールの脂肪酸エステ
ル類が使用されてきた。In order to satisfy these demands, esters of mineral oils, higher alcohols and fatty acids, and esters of dibasic acids such as adipic acid and sebacic acid have been used as lubricant components that are blended with emulsifiers, antistatic agents, etc. Fatty acid esters of polyhydric alcohols such as trimethylolpropane, glycerin, etc. have been used.
しかしながら、そのような従来から使用されてきている
処理油剤は良好な平滑性を示すものの、熱延伸時や仮撚
加工工程等の特に苛酷な加熱工程を経る熱可塑性合成繊
維糸条に対しては耐熱性が十分でなく、発煙して作業環
境を悪化させたり、ヒーター上でタール状物質を形成し
て糸道の汚れが顕著となり、単糸巻き付きや糸切れが発
生したりする。However, although such conventionally used processing oils exhibit good smoothness, they are not suitable for thermoplastic synthetic fiber yarns that undergo particularly severe heating processes such as hot drawing and false twisting processes. It does not have sufficient heat resistance and may emit smoke, worsening the working environment, or form tar-like substances on the heater, making the thread path noticeably dirty and causing single thread wrapping and thread breakage.
その結果、円滑な延伸や仮撚加工が行えなくなり、機械
の運転を停止し、清掃してタール状物質を取り除かなけ
ればならず、工程上のトラブルを起こしたり、能率低下
をきたしていた。As a result, smooth stretching and false twisting cannot be performed, and the machine must be stopped and cleaned to remove the tar-like substance, causing process troubles and reducing efficiency.
更に、最近の繊維製造工程の高速化とあいまって、繊維
製造メーカーが立地している地域の環境保全(例えば、
発煙によるエアポリューションの問題等)を強化する要
請が益々強くなっており、処理用油剤のなお一層の耐熱
性向上を要することとなった。Furthermore, with the recent speeding up of textile manufacturing processes, environmental conservation in the regions where textile manufacturers are located (e.g.
There is an increasingly strong demand for improving the heat resistance of treatment oils, as there is an increasing demand for improvements in the problem of air pollution caused by smoke generation, etc.
そこでこの様な状況に鑑み、本発明者らは加熱工程にお
ける発煙やタール状物質の亜酸を抑えるべく鋭意検討を
重ねた結果、特定のエステル化合物を含有する合成繊維
処理用油剤を用いれば上記の問題点の生しないことを見
出し、本発明を完成するに至った。In view of this situation, the inventors of the present invention have conducted intensive studies to suppress smoke generation during the heating process and the generation of subacids in tar-like substances.The inventors of the present invention have found that using a synthetic fiber processing oil containing a specific ester compound will eliminate the above-mentioned problems. The inventors have discovered that the above problems do not occur and have completed the present invention.
すなわち本発明は、下記一般式+11
(式中、R,、R,はそれぞれ独立に炭素数1〜4のア
ルキレン基を表す。)
で表される2価アルコールと、炭素数8〜24ノ脂肪酸
とのエステルを必須成分とする熱可塑性合成繊維処理用
油剤を提供するものである。That is, the present invention provides a dihydric alcohol represented by the following general formula +11 (in the formula, R, , R, each independently represents an alkylene group having 1 to 4 carbon atoms) and a fatty acid having 8 to 24 carbon atoms. The present invention provides an oil agent for treating thermoplastic synthetic fibers containing an ester of
上記エステルの原料となる2価アルコールとしては、
上記エステルの原料となる炭素数8〜24の脂肪酸とし
ては、2−エチルヘキサン酸、n−オクタン酸、カプリ
ン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステ
アリン酸、イソステアリン酸、オレイン酸、エルカ酸等
が挙げられる。脂肪酸の炭素数が8より小さい場合には
発煙防止性が不良となり、また24より大きい場合には
タール化が問題となったり、平滑性が不良となったりす
る。Dihydric alcohols that are raw materials for the above esters include 2-ethylhexanoic acid, n-octanoic acid, capric acid, lauric acid, myristic acid, and palmitic acid. , stearic acid, isostearic acid, oleic acid, erucic acid, and the like. If the number of carbon atoms in the fatty acid is less than 8, the smoke prevention property will be poor, and if it is more than 24, there will be a problem of tar formation or poor smoothness.
本発明の前記エステルは一般式+1+で表される2価ア
ルコールと上記脂肪酸とをエステル化反応させることに
よって得られる。本発明の合成繊維処理用油剤中の該エ
ステルの含有量は特に限定されないが、20重量%以上
であることが好ましい。The ester of the present invention can be obtained by subjecting the dihydric alcohol represented by the general formula +1+ to an esterification reaction with the fatty acid. The content of the ester in the synthetic fiber treatment oil of the present invention is not particularly limited, but is preferably 20% by weight or more.
本発明の熱可塑性合成繊維処理用油剤には必要に応じて
公知の潤滑剤(例えば、ラウリルオレート、オレイルオ
レートの如き脂肪族モノエステル類;ジオレイルアジペ
ート、ジオクチルフタレート、エチレングリコールジオ
レート等の二塩基酸ジエステル類及び二価アルコールジ
エステル類;トリメチロールプロパントリラウレート、
グリセリントリオレート、ペンタエリスリトールテトラ
オレートの如き多価アルコールエステル頻;トリイソス
テアリルトリメリテート等の多塩基酸エステル)や、ポ
リオキシエチレンソルビタンエステル、硬化ヒマシ油の
酸化エチレン付加物、高級アルコール酸化エチレン付加
物、高級脂肪酸酸化エチレン付加物等の乳化剤、更には
アルキルホスフェートカリ塩、オレイン酸カリ、イ旦ダ
ソリン型両性活性剤、ベタイン型両性活性剤等の帯電防
止剤を配合することができる。The oil for treating thermoplastic synthetic fibers of the present invention may include known lubricants (for example, aliphatic monoesters such as lauryl oleate and oleyl oleate; dioleyl adipate, dioctyl phthalate, and ethylene glycol diolate) as necessary. Basic acid diesters and dihydric alcohol diesters; trimethylolpropane trilaurate,
polyhydric alcohol esters such as glycerin triolate and pentaerythritol tetraolate; polybasic acid esters such as triisostearyl trimellitate), polyoxyethylene sorbitan esters, ethylene oxide adducts of hydrogenated castor oil, and higher alcohol ethylene oxides. Emulsifiers such as adducts, higher fatty acid ethylene oxide adducts, and antistatic agents such as alkyl phosphate potassium salts, potassium oleate, dasoline-type amphoteric surfactants, and betaine-type amphoteric surfactants can be added.
斯くして得られた、本発明の熱可塑性合成繊維処理用油
剤は、常法により水中に乳化して水性エマルジョンとし
たり、低粘度の希釈溶剤に溶解してオイリングローラ一
方式、スプレー法、ノズルオイリング方式等により、繊
維糸条に対し0.2ないし2.0重量%給油される。The thus obtained oil agent for treating thermoplastic synthetic fibers of the present invention can be emulsified in water to form an aqueous emulsion by a conventional method, or dissolved in a low viscosity diluting solvent and used with an oiling roller, a spray method, or a nozzle. The fiber threads are oiled in an amount of 0.2 to 2.0% by weight using an oiling method or the like.
本発明の処理剤は耐熱性、平滑性、サイジング性に優れ
ているという特徴を有している為、これら特徴を生かし
たものであれば、糊付糸川原糸処理剤、加工糸油剤、無
糊系用油剤、トリコット用油剤、タイヤコード油剤等の
平滑剤成分としても用いることができる。The processing agent of the present invention has the characteristics of being excellent in heat resistance, smoothness, and sizing properties, so if it takes advantage of these characteristics, it can be used as a sized Itokawa yarn processing agent, a processed yarn oil agent, or a non-sizing agent. It can also be used as a smoothing agent component in adhesive oils, tricot oils, tire cord oils, and the like.
〔発明の効果〕
本発明の熱可塑性合成繊維処理用油剤で処理された熱可
塑性合成繊維は、非常に優れた強力低下防止性を示し、
熱伸延あるいは熱固定工程において160°Cないし2
50″Cに加熱されたヒータープレート上あるいはロー
ラー上でタール状物質を生成して作業能率を低下させた
りすることはない。また、潤滑性においても従来から使
用されているものと同様良好な潤滑性を示す。[Effects of the Invention] The thermoplastic synthetic fibers treated with the thermoplastic synthetic fiber processing oil of the present invention exhibit extremely excellent strength loss prevention properties,
160°C or 2°C during heat stretching or heat setting process
It does not generate tar-like substances on the heater plate heated to 50"C or on the rollers, reducing work efficiency. Also, the lubrication property is as good as that used conventionally. Show your gender.
以下、実施例をもって本発明を説明するが、本発明はこ
れら実施例に限定されるものではない。The present invention will be explained below with reference to Examples, but the present invention is not limited to these Examples.
実施例1
下記−形式+l[)で表されるエステル化合物のRlR
t、 Rs、 R4がそれぞれ表−1に示すようなエス
テル化合物及びエステル化合物A、Bを用いて本発明の
熱可塑性合成繊維処理用油剤1〜7を調製し、それぞれ
の耐熱性評価及び摩擦測定を以下の方法によって行った
。Example 1 RlR of an ester compound represented by the following -format +l[)
Oils 1 to 7 for treating thermoplastic synthetic fibers of the present invention were prepared using ester compounds and ester compounds A and B in which t, Rs, and R4 are shown in Table 1, respectively, and the heat resistance evaluation and friction measurement were conducted for each oil agent. was carried out using the following method.
また、比較品として表−2に示すような従来より使用さ
れている公知の収録を用いた熱可塑性合成繊維処理用油
剤8〜12を調製し、同様の試験を行った。In addition, as comparison products, oil agents 8 to 12 for treating thermoplastic synthetic fibers were prepared using conventionally used known recordings as shown in Table 2, and similar tests were conducted.
エステル化合物A
エステル化合物B
表
「
油
剤
戒
分
】
注):
*化合物C
:ラウリン酸残基
(1)耐熱性試験
(i)ガードナー法による試料の色の判定SUS Fi
に直径25m5.深さ5+nmの凹みをっけ、その中に
各評価用油剤100 tiを滴下し、試料温度240
’Cで10分間ヒータープレート上で加熱した後、ガー
ドナー法により色の判定を行う。Ester compound A Ester compound B Table "Oil agent precepts" Note): *Compound C: Lauric acid residue (1) Heat resistance test (i) Judgment of sample color by Gardner method SUS Fi
diameter 25m5. Make a dent with a depth of 5+ nm, drop 100 ti of each evaluation oil into the dent, and set the sample temperature to 240 ml.
After heating on a heater plate for 10 minutes at 'C, the color is determined by the Gardner method.
(ii )タール化率の測定
市販のアルミニウム皿に各評価用油剤を約0.5g採取
し、これを熱風式乾燥器に入れ、250°Cで4時間加
熱後取り出す。室温に放冷後アセトンで該アルミニウム
皿を洗浄する。(ii) Measurement of tar rate: Approximately 0.5 g of each evaluation oil was collected in a commercially available aluminum dish, placed in a hot air dryer, heated at 250°C for 4 hours, and then taken out. After cooling to room temperature, wash the aluminum dish with acetone.
一般にアセトンに溶解しない残存試料は黒色の樹脂化し
た物質で、この量の多い程タール化率が大きい。Generally, the remaining sample that does not dissolve in acetone is a black resinous substance, and the larger the amount, the higher the rate of taring.
尚、タール化率は以下の式によって計算した。Incidentally, the tar rate was calculated using the following formula.
タール化率(%)=
床取した試料の■盟(g)
(2)対金属摩擦試験
評価用油剤1〜lOを、市販の1260 dのナイロン
タイヤコード糸を脱油し乾燥して得た糸に1%付着させ
、走行糸法で200°Cにおける対金属摩擦係数を測定
した。Tar conversion rate (%) = ◯ (g) of the sample taken from the floor (2) Oil agent 1 to 10 for evaluation of friction against metal test was obtained by deoiling and drying a commercially available 1260 d nylon tire cord thread. It was attached to a thread at 1%, and the coefficient of friction against metal at 200°C was measured using the running thread method.
これらの結果を表−3に示す。These results are shown in Table 3.
箱二、藍
表−3に示す結果より、本発明の熱可塑性合成繊維処理
用油剤は比較品に比べ非常に優れた耐熱性を示し、ター
ル状物質を形成しないことがわかる。また摩擦係数、す
なわち潤滑性についても従来から使用されている油剤と
同様に良好である。Box 2, Indigo The results shown in Table 3 show that the oil agent for treating thermoplastic synthetic fibers of the present invention exhibits extremely superior heat resistance compared to comparative products and does not form tar-like substances. Furthermore, the coefficient of friction, that is, the lubricity, is as good as that of conventionally used oils.
Claims (1)
のアルキレン基を表す。) で表される2価アルコールと、炭素数8〜24の脂肪酸
とのエステルを必須成分とする熱可塑性合成繊維処理用
油剤。[Claims] 1 The following general formula (1) ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (In the formula, R_1 and R_2 each independently have a carbon number of 1 to 4.
represents an alkylene group. ) An oil agent for treating thermoplastic synthetic fibers containing an ester of a dihydric alcohol represented by the following formula and a fatty acid having 8 to 24 carbon atoms as an essential component.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16288189A JPH0333267A (en) | 1989-06-26 | 1989-06-26 | Finishing oil for treating thermoplastic synthetic fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16288189A JPH0333267A (en) | 1989-06-26 | 1989-06-26 | Finishing oil for treating thermoplastic synthetic fiber |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0333267A true JPH0333267A (en) | 1991-02-13 |
Family
ID=15763039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16288189A Pending JPH0333267A (en) | 1989-06-26 | 1989-06-26 | Finishing oil for treating thermoplastic synthetic fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0333267A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006306773A (en) * | 2005-04-28 | 2006-11-09 | New Japan Chem Co Ltd | Alicyclic dihydric alcohol ester |
JP2006306987A (en) * | 2005-04-28 | 2006-11-09 | New Japan Chem Co Ltd | Lubricating oil |
-
1989
- 1989-06-26 JP JP16288189A patent/JPH0333267A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006306773A (en) * | 2005-04-28 | 2006-11-09 | New Japan Chem Co Ltd | Alicyclic dihydric alcohol ester |
JP2006306987A (en) * | 2005-04-28 | 2006-11-09 | New Japan Chem Co Ltd | Lubricating oil |
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